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Submission Tags: falconsandbox
Submission: On October 30 via api from US — Scanned from DE
Submission Tags: falconsandbox
Submission: On October 30 via api from US — Scanned from DE
Form analysis 1 forms found in the DOM
<form id="search-form" class="usa-search usa-search-big" data-disable-change-monitor="true">
<label class="usa-sr-only" for="search-field-big">Enter sequence type</label>
<input id="search-field-big" name="search" type="search" placeholder="Enter sequence type" autocomplete="off">
<button id="clear-btn" class="ncbi-clear-button-x" type="reset" aria-controls="search_term" aria-hidden="false"><span class="fa fa-times"></span><span class="usa-sr-only">Clear</span></button>
<button id="search-btn" type="submit"><i class="fa fa-search" aria-hidden="true"></i><span class="usa-search-submit-text">Suggest tool</span></button>
<div id="suggested-tools" class="suggestions">
<h3>Suggested tools</h3>
<ul id="suggested-tools-ul" class="usa-font-lead">
<li id="tool-sra-item">
<a href="/about/sra/" class="link-arrow"><span>SRA</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p> SRA accepts unassembled reads from high throughput sequencing platforms. Submitted data files should generally be minimally processed and include per-base quality scores. </p>
</li>
<li id="tool-srasars-item">
<a href="/sarscov2/sra/" class="link-arrow"><span>SRA</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p> Submit unassembled reads of SARS-CoV-2 with BioProject, BioSample, metadata and NGS files. </p>
</li>
<li id="tool-geo-item">
<a href="https://www.ncbi.nlm.nih.gov/geo/info/submission.html" class="link-arrow"><span>GEO</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p> GEO accepts raw data, processed data and metadata for gene expression and epigenomics datasets generated by high-throughput sequencing and microarray technologies. </p>
</li>
<li id="tool-genome-item">
<a href="/about/genome/" class="link-arrow"><span>Genome</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Submit assembled complete or incomplete/draft prokaryotic and eukaryotic genomes. Not for viral, phage, or single locus sequences (for example: 16S rRNA). Submit those to regular <a href="https://www.ncbi.nlm.nih.gov/WebSub/">GenBank</a>.
</p>
</li>
<li id="tool-tsa-item">
<a href="/about/tsa/" class="link-arrow"><span>TSA</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p> Computationally assembled transcribed RNA sequences representing a transcriptome derived from sequence reads submitted to Sequence Read Archive (SRA). </p>
</li>
<li id="tool-genbank-item">
<a href="/about/genbank/" class="link-arrow"><span>GenBank</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Submit ribosomal RNA (rRNA), rRNA-ITS, SARS-CoV-2, Influenza, Norovirus, Dengue, metazoan COX1 or eukaryotic nuclear mRNA</p>
</li>
<li id="tool-genbanksars-item">
<a href="/sarscov2/genbank/" class="link-arrow"><span>GenBank</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Submit assembled reads of SARS-CoV-2 with FASTA files and source metadata. Annotation for SARS-CoV-2 is not required.</p>
</li>
<li id="tool-genbankmrna-item">
<a href="/about/genbank/" class="link-arrow"><span>GenBank</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Eukaryotic nuclear mRNAs (limit 499 sequences)</p>
</li>
<li id="tool-bankitmrna-item">
<a href="/about/bankit/" class="link-arrow"><span>BankIt</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>other mRNAs</p>
</li>
<li id="tool-bankit-item">
<a href="/about/bankit/" class="link-arrow"><span>BankIt</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Submit genomic DNA, organelle, ncRNA, plasmids, other viruses, phages, mRNA and synthetic constructs.</p>
</li>
<li id="tool-dbgap-item">
<a href="/dbgap/" class="link-arrow"><span>dbGaP</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Microarray data from clinical studies that require controlled access.</p>
</li>
<li id="tool-clinvar-item">
<a href="/clinvar/" class="link-arrow"><span>ClinVar</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Information on human sequence variation and relationship to human health.</p>
</li>
<li id="tool-nihms-item">
<a href="https://nihms.nih.gov/" class="link-arrow"><span>NIHMS</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Submit the electronic version of a peer-reviewed manuscript for inclusion in PubMed Central.</p>
</li>
<li id="tool-clinicaltrialsgov-item">
<a href="https://clinicaltrials.gov/" class="link-arrow"><span>ClinicalTrials.gov</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Explore clinicial studies conducted around the world.</p>
</li>
<li id="tool-tls-item">
<a href="/about/tls/" class="link-arrow"><span>TLS</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Large-scale sequencing projects for an individual loci are taken in GenBank & Sequence Read Archive (SRA).</p>
</li>
<li id="tool-suppfiles-item">
<a href="/subs/supfiles/" class="link-arrow"><span>Supplementary Files</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Submit BioNano maps, Beta-lactamase gene, and PacBio methylation data.</p>
</li>
<li id="tool-tpa-item">
<a href="https://www.ncbi.nlm.nih.gov/genbank/tpa/" class="link-arrow"><span>Third Party Annotation (TPA)</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>NCBI takes data capturing experimental or inferential results supporting annotation dervied from GenBank primary data.</p>
</li>
<li id="tool-dbsnp-item">
<a href="/subs/variation_org/" class="link-arrow"><span>dbSNP</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Small human genomic variation: single nucleotide, insertions, deletions, and microsatellites.</p>
</li>
<li id="tool-gtr-item">
<a href="/subs/gtr/" class="link-arrow"><span>GTR</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Genetic tests for inherited & somatic genetic variations, including arrays and multiplex panels.</p>
</li>
<li id="tool-bpbs-item">
<a href="/about/bioproject-biosample/" class="link-arrow"><span>BioProject and BioSample</span> <i class="fa fa-angle-right" aria-hidden="true"></i></a>
<p>Automatically create a BioProject and BioSample during sequence data submission.</p>
</li>
</ul>
</div>
<div id="suggest-error" class="suggestions">
<h3>No results found</h3>
<p class="usa-font-lead"> We need a little more information. Add to your description above, indicating sequence data type and/or whether your data is assembled, unassembled or expression data. </p>
</div>
<ul id="suggest-hotlinks" class="usa-font-lead">
<li><a class="usa-label" href="sarscov2/">SARS-CoV-2</a></li>
<li><a class="usa-label">16S rRNA</a></li>
<li><a class="usa-label">genome</a></li>
<li><a class="usa-label">ITS</a></li>
<li><a class="usa-label">SRA</a></li>
</ul>
</form>Text Content
Skip to main page content An official website of the United States government Here's how you know The .gov means it’s official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site. The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. Log in Show account info Close ACCOUNT Logged in as: username * Dashboard * Publications * Account settings * Log out Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation * Submission Portal Menu Close * Submission Portal SUBMISSION PORTAL Submit to the world's largest public repository of biological and scientific information Type a few words about the sequence data you are submitting and select an option to learn more. You can also browse submission information below. WHAT DO YOU WANT TO SUBMIT? Enter a few words about your sequence data. Enter sequence type Clear Suggest tool SUGGESTED TOOLS * SRA SRA accepts unassembled reads from high throughput sequencing platforms. Submitted data files should generally be minimally processed and include per-base quality scores. * SRA Submit unassembled reads of SARS-CoV-2 with BioProject, BioSample, metadata and NGS files. * GEO GEO accepts raw data, processed data and metadata for gene expression and epigenomics datasets generated by high-throughput sequencing and microarray technologies. * Genome Submit assembled complete or incomplete/draft prokaryotic and eukaryotic genomes. Not for viral, phage, or single locus sequences (for example: 16S rRNA). Submit those to regular GenBank. * TSA Computationally assembled transcribed RNA sequences representing a transcriptome derived from sequence reads submitted to Sequence Read Archive (SRA). * GenBank Submit ribosomal RNA (rRNA), rRNA-ITS, SARS-CoV-2, Influenza, Norovirus, Dengue, metazoan COX1 or eukaryotic nuclear mRNA * GenBank Submit assembled reads of SARS-CoV-2 with FASTA files and source metadata. Annotation for SARS-CoV-2 is not required. * GenBank Eukaryotic nuclear mRNAs (limit 499 sequences) * BankIt other mRNAs * BankIt Submit genomic DNA, organelle, ncRNA, plasmids, other viruses, phages, mRNA and synthetic constructs. * dbGaP Microarray data from clinical studies that require controlled access. * ClinVar Information on human sequence variation and relationship to human health. * NIHMS Submit the electronic version of a peer-reviewed manuscript for inclusion in PubMed Central. * ClinicalTrials.gov Explore clinicial studies conducted around the world. * TLS Large-scale sequencing projects for an individual loci are taken in GenBank & Sequence Read Archive (SRA). * Supplementary Files Submit BioNano maps, Beta-lactamase gene, and PacBio methylation data. * Third Party Annotation (TPA) NCBI takes data capturing experimental or inferential results supporting annotation dervied from GenBank primary data. * dbSNP Small human genomic variation: single nucleotide, insertions, deletions, and microsatellites. * GTR Genetic tests for inherited & somatic genetic variations, including arrays and multiplex panels. * BioProject and BioSample Automatically create a BioProject and BioSample during sequence data submission. NO RESULTS FOUND We need a little more information. Add to your description above, indicating sequence data type and/or whether your data is assembled, unassembled or expression data. * SARS-CoV-2 * 16S rRNA * genome * ITS * SRA GENBANK GenBank is the world's largest nucleotide archive containing sequences from all branches of life. The archive is a foundation for medical and biological discovery. * Submit assembled SARS-CoV-2, Influenza, Norovirus, Dengue virus, rRNA, rRNA-ITS, metazoan COX1, Eukaryotic nuclear mRNA sequences. Learn moreSubmit * Submit genomic DNA, organelle, ncRNA, plasmids, other viruses, phages, other mRNA, synthetic constructs. Learn moreSubmit * Submit assembled prokaryotic and eukaryotic genomes. Learn moreSubmit SEQUENCE READ ARCHIVE (SRA) SRA is the largest publicly-available repository of high throughput sequencing data. The archive accepts data from all branches of life as well as metagenomic and environmental surveys. * Submit unassembled, high throughput sequencing reads SARS-CoV-2 submission instructions Learn more Submit OTHER TOOLS * TSA Submit computationally assembled, transcribed RNA sequences after submitting unassembled reads to SRA. Learn more * GEO Submit RNA-seq, ChIP-seq, and other types of gene expression and epigenomics datasets. Learn more * BIOPROJECT & BIOSAMPLE Choose a tool above if submitting sequence data. Learn more SEQUENCE SUBMISSION FAQ * WHAT IS AN ACCESSION NUMBER? An accession number in bioinformatics is a unique identifier given to a DNA or protein sequence record to allow for tracking of different versions of that sequence record and the associated sequence over time in a single data repository. Because of its relative stability, accession numbers can be utilized as foreign keys for referring to a sequence object, but not necessarily to a unique sequence. All sequence information repositories implement the concept of "accession number" but might do so with subtle variation. * WHAT HAPPENS AFTER MY DATA IS SUBMITTED? Please read the NLM GenBank and SRA Data Processing document which describes how sequence data are processed and made available to the public, responsibilities of the data submitter, responsibilities of NCBI, and defines data status. You may write to info@ncbi.nlm.nih.gov if you have questions about your submitted data or if you have questions about the document. MEDICAL GENETICS & VARIATION TOOLS Submit clinical data, small & large human genomics variants, and genotype & phenotype data. * ClinVar * GTR * Variation * dbGaP OTHER RESOURCES * Clinical Trials * Manuscripts Follow NCBI Twitter Facebook LinkedIn GitHub Connect with NLM * Twitter * SM-Facebook * SM-Youtube National Library of Medicine 8600 Rockville Pike Bethesda, MD 20894 Web Policies FOIA HHS Vulnerability Disclosure Help Accessibility Careers * NLM * NIH * HHS * USA.gov PLEASE TELL US ABOUT YOUR VISIT! Form Approved OMB# 0925-0648 Exp. Date7/31/2027 Start SurveyNo Thanks